Gene test breakthrough for mysterious childhood epilepsy?
NCT ID NCT03652246
First seen Mar 22, 2026 · Last updated May 16, 2026 · Updated 9 times
Summary
This pilot study tested a new, faster genetic test (exome sequencing) on 15 patients with severe epilepsy and developmental delays of unknown cause. The goal was to see if this test could find more genetic answers than standard methods, which could improve genetic counseling for families. The study focused on patients with suspected inherited forms of the condition.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Chu Dijon Bourogne
Dijon, 21000, France
Conditions
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